Orbital and nasolacrimal disorders and retinoblastoma in children


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Abstract

Recent publications concerning congenital craniofacial anomalies, orbital proptosis, anophthalmic socket, congenital nasolacrimal duct obstruction, and retinoblastoma are reviewed. Congenital craniofacial anomalies are rare conditions often presenting challenging diagnostic and reconstructive problems which require coordinated management by a team of specialists. More ophthalmologists are invited to venture into this peripheral area of ophthalmology. Prenatal screening and carrier detection using restriction fragment length polymorphisms will have a major influence in the clinical management of retinoblastoma.

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